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210922s2021 xx |||||o 00| ||eng c |
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|a (DE-627)WHO007904649
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|a (UBBS_Klinische_Studien_WHO)EUCTR2021-003386-35-ES
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|a (UBBS_Klinische_Studien_WHO)INSIGHT-016
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|a DE-627
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|e rakwb
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|a eng
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|a Vaccination for Recovered Inpatients with COVID-19 (VATICO)
|b SARS-CoV-2 vaccination strategies in previous hospitalised and recovered COVID-19 patients - VATICO
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|c 2021
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|a Text
|b txt
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|a Computermedien
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|a Online-Ressource
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 26-07-2021, Last updated: 2022-11-24
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|a Medical Condition: Participants of the ACTIV-3/TICO clinical trial at selected sites who received certain pre-specified blinded investigational agents or placebo as part of that trial, and who have since achieved sustained recovery, and who are still [TICO assignment] blinded, and who are still within 28 to 90 days after initial TICO randomization, will be randomized in this 2x2 factorial design to one of four groups of the Moderna mRNA 1273 or the Pfizer BNT162b2 vaccine (mRNA vaccines) MedDRA version: 23.1Level: LLTClassification code 10084465Term: COVID-19 vaccinationSystem Organ Class: 100000004865;Therapeutic area: Health Care [N] - Environment and Public Health [N06]
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|a Study Type: Interventional
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|a Phase: Phase 4
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|a Recruitment Status: Authorised-recruitment may be ongoing or finished
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|a 610
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|i Enthalten in
|t WHO International Clinical Trials Registry Platform
|g (2021) vom: 13. Sept.
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|g year:2021
|g day:13
|g month:09
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|u https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2021-003386-35
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|a GBV_CTG
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912 |
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|a SSG-OLC-PHA
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|a AR
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|j 2021
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